Efficacy and Safety of Belumosudil in Subjects With Diffuse Cutaneous Systemic Sclerosis

NCT ID: NCT04680975

Last Updated: 2023-06-05

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-03-03
• Study Completion Date: 2022-12-19

Brief Summary

This was a phase 2, open-label, single-cohort, multicenter trial of belumosudil in participants with Diffuse Cutaneous Systemic Sclerosis (dcSSc). An estimated total of 12 to 15 participants would receive belumosudil 200 milligrams (mg) administered orally (PO) twice daily (BID) for 52 weeks. The primary analysis was at 24 weeks.

Detailed Description

The primary objective of this phase 2, open-label, single-cohort, multicenter trial was to evaluate the efficacy of belumosudil 200 mg BID using the Combined Response Index in diffuse cutaneous Systemic Sclerosis (CRISS) after 24 weeks of therapy. The duration of the study was approximately 14 months (4 weeks for screening, 52 weeks of dosing period, and 4 weeks of Follow-up)

Participants who had signed an Institutional Review Board/Independent Ethics Committee-(IRB/IEC)-approved informed consent form (ICF) and met all of the inclusion/exclusion criteria were enrolled. A total of 10 participants at 6 sites received belumosudil 200 mg in tablet form administered PO BID for 52 weeks. The total duration of the study is approximately 14 months: a 4-week screening period, a 52-week treatment period, and a 4-week follow-up.

The primary endpoint was analyzed using Week 24 data.

Efficacy was assessed throughout the 52-week dosing period using:

• Composite Response Index in Systemic Sclerosis (CRISS)
• Modified Rodnan Skin Score (mRSS)
• Pulmonary Function Tests (PFTs)
• Physician Global Assessment
• Patient Global Assessment

Safety was be assessed throughout the study and will include:.

• Physical examinations (PEs)
• Vital sign measurements
• Weight measurements
• Blood sample collection for hematology and chemistry; urinalysis
• Electrocardiograms (ECGs)
• Adverse event (AE) assessments
• Concomitant medication assessments
• Pregnancy testing for females of childbearing potential.

Reasons for discontinuation of treatment because of adverse events were documented. Careful monitoring of all adverse events was carried out. Dosing could be reduced 1 dose level. If the dose was not tolerated, then the participant was discontinued from the study. If there is an interruption of dosing, after 14 days the participant was discontinued from the study.

Participants were given a study drug diary to record the details of each dose of belumosudil 200 mg. Diaries were dispense/collected on each visit. Compliance with dosing was confirmed using participant diaries, which was examined at each visit by site staff to determine if dosing was as instructed per protocol and follow-up.

A 4-Week Safety Follow-up Visit occurred 28 days (± 3 days) after the last dose of study drug.

Conditions

Diffuse Cutaneous Systemic Sclerosis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Belumosudil

Participants received belumosudil 200 mg tablet orally PO, BID for 52 weeks.

Group Type: EXPERIMENTAL

Belumosudil

Intervention Type: DRUG

10 participants with dcSSc received belumosudil 200 mg PO BID for 52 weeks

Interventions

Belumosudil

10 participants with dcSSc received belumosudil 200 mg PO BID for 52 weeks

Intervention Type: DRUG

Other Intervention Names

KD025

Eligibility Criteria

Inclusion Criteria

1. Male and female participants greater than or equal to (>=) 18 years old with the diagnosis of dcSSc according to the 2013 American College of Rheumatology and European League Against Rheumatism.

2. Had disease duration (defined as interval from first non Raynaud disease manifestation) of less than or equal to (<=) 6 years.

3. Had mRSS of >=15 but <=40.

4. Had active disease as determined by the Principal Investigator within the 6 months prior to screening.

5. Adequate organ and bone marrow functions evaluated during the 28 days prior to enrollment as follows:

1. Absolute neutrophil count >= 1.5*10^9/L

2. Platelet count >= 100*10^9/L

3. Total bilirubin <= 1.0*upper limit of normal (ULN)

4. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST), and serum creatinine <= 1.5*ULN.

6. Female participants of childbearing potential had a negative pregnancy test at screening. Females of childbearing potential were defined as sexually mature women without prior hysterectomy or who had any evidence of menses in the past 12 months. However, women who had been amenorrheic for 12 or more months were still considered to be of childbearing potential if the amenorrhea was possibly due to prior chemotherapy, anti-estrogens, or ovarian suppression.

1. Women of childbearing potential (i.e., menstruating women) must had a negative urine pregnancy test (positive urine tests were to be confirmed by serum test) documented within the 24-hour period prior to the first dose of study drug.

2. Sexually active women of childbearing potential enrolled in the study agreed to use two forms of accepted methods of contraception during the course of the study and for 3 months after their last dose of study drug. Effective birth control includes (i) intrauterine device plus 1 barrier method; (ii) on stable doses of hormonal contraception for at least 3 months (e.g., oral, injectable, implant, transdermal) plus 1 barrier method; or (iii) 2 barrier methods. Effective barrier methods are male or female condoms, diaphragms, and spermicides (creams or gels that contain a chemical to kill sperm), or a vasectomized partner.

7. For male participants who were sexually active and who were partners of premenopausal women: agreement to use 2 forms of contraception as in criterion number 6b above during the treatment period and for at least 3 months after the last dose of study drug.

8. Male participants must not donate sperm for 3 months after last dose of study drug.

9. Able to provide written informed consent prior to the performance of any study-specific procedures.

Exclusion Criteria

1. Participants had corrected QT interval using Fridericia's formula (QTcF) greater than 450 milliseconds.

2. Ongoing use or current use of concomitant medication known to have the potential for QTc prolongation.

3. Female participant who was pregnant or breastfed.

4. Participated in another study with an investigational drug within 28 days of study entry (for studies involving biologics, within 3 half-lives of the biologic).

5. History or other evidence of severe illness or any other conditions that would make the participant, in the opinion of the Investigator, unsuitable for the study.

6. Chronic heart failure with New York Heart Association Classes II, III, or IV.

7. Acute or chronic liver disease (e.g., cirrhosis).

8. Positive human immunodeficiency virus (HIV) test.

9. Active hepatitis C virus (HCV), hepatitis B virus (HBV), or positive whole blood tuberculin test.

10. Diagnosed with any malignancy within 3 years of enrollment, with the exception of basal cell or completely resected squamous cell carcinoma of the skin, resected in situ cervical malignancy, resected breast ductal carcinoma in situ, or low risk prostate cancer after curative resection.

11. Had previous exposure to belumosudil or known allergy/sensitivity to belumosudil, or any other Rho-associated Protein Kinase-2 (ROCK2) inhibitor.

12. Scleroderma renal crisis within 4 months prior to enrollment.

13. Forced vital capacity <= 50% Predicted.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Kadmon, a Sanofi Company

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University of California, Los Angeles Medical Center_Site number 104

Los Angeles, California, United States

Yale University School of Medicine_Site number 140

New Haven, Connecticut, United States

Northwestern University_Site number 124

Chicago, Illinois, United States

Columbia University Medical Center_Site number 086

New York, New York, United States

University of Utah_Site number 048

Salt Lake City, Utah, United States

Virginia Mason Medical Center_Site number 145

Seattle, Washington, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

KD025-215

Identifier Type: OTHER

Identifier Source: secondary_id

ACT17634

Identifier Type: -

Identifier Source: org_study_id